Ccrp Angie Kimbler angie.kimbler@resilience.com & & +1 617-245-0512 | Certified Clinical Research Professional (CCRP) with a BS in Clinical Research and over 20 years of experience in clinical research. Over ten years of experience conducting clinical research at investigative sites as a clinical research coordinator and regulatory affairs specialist. Ten years of experience in the biopharmaceutical industry supporting clinical research by ensuring successful day to day clinical operations and support for regulatory submissions such as Investigational New Drug Applications, Drug Master Files, and 510ks. Knowledge and experience in the application of FDA guidelines and the US Code of Federal Regulations in relations to Current Good Clinical Practices (cGCP) and Current Good Manufacturing Practices (GMP). Current responsibilities include ensuring that all clinical trial projects are properly resourced, managed, and executed within budget and in accordance with established timelines and quality standards. Manage the day to day clinical operations, including the management of vendors and coordination of activities. Ensure that all clinical trials are executed in compliance with cGCP guidelines, FDA regulations, and company standard operating procedures.

Ccrp Angie Kimbler

Certified Clinical Research Professional (CCRP) with a BS in Clinical Research and over 20 years of experience in...

Gainesville, Florida, United States

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Ccrp Angie Kimbler’s Emails [email protected]

Ccrp Angie Kimbler’s Phone Numbers 1617245****

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Ccrp Angie Kimbler’s Location Gainesville, Florida, United States

Ccrp Angie Kimbler’s Expertise Certified Clinical Research Professional (CCRP) with a BS in Clinical Research and over 20 years of experience in clinical research. Over ten years of experience conducting clinical research at investigative sites as a clinical research coordinator and regulatory affairs specialist. Ten years of experience in the biopharmaceutical industry supporting clinical research by ensuring successful day to day clinical operations and support for regulatory submissions such as Investigational New Drug Applications, Drug Master Files, and 510ks. Knowledge and experience in the application of FDA guidelines and the US Code of Federal Regulations in relations to Current Good Clinical Practices (cGCP) and Current Good Manufacturing Practices (GMP). Current responsibilities include ensuring that all clinical trial projects are properly resourced, managed, and executed within budget and in accordance with established timelines and quality standards. Manage the day to day clinical operations, including the management of vendors and coordination of activities. Ensure that all clinical trials are executed in compliance with cGCP guidelines, FDA regulations, and company standard operating procedures.

Ccrp Angie Kimbler’s Current Industry Resilience

Ccrp Angie Kimbler’s Prior Industry
Clin Sci International | Amk Research | Nanotherapeutics | Ology Bioservices | Resilience

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Work Experience

Resilience

Sr. Manager, Regulatory & Clinical Operations

Thu Apr 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Present

Ology Bioservices

Sr. Manager, Clinical & Regulatory Operations

Fri Sep 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Apr 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)

Nanotherapeutics

Sr. Manager, Regulatory and Clinical Operations

Sat Jul 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Sep 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)

Nanotherapeutics

Director, Clinical Operations

Mon Apr 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jun 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)

Nanotherapeutics

Clinical Trials Manager

Wed Aug 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Apr 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time)

Nanotherapeutics

Office Manager

Fri Sep 01 2006 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Aug 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time)

Amk Research

Cheif Operating Office

Fri Aug 01 2003 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Sep 01 2006 00:00:00 GMT+0000 (Coordinated Universal Time)

Clin Sci International

Chief Operating Officer

Mon Jan 01 2001 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Jan 01 2003 00:00:00 GMT+0000 (Coordinated Universal Time)

Skills

Languages

FAQ About Ccrp Angie Kimbler

Ccrp Angie Kimbler is located at
Gainesville, Florida, United States

Ccrp Angie Kimbler is a
Certified Clinical Research Professional (CCRP) with a BS in Clinical Research and over 20 years of experience in clinical research. Over ten years of experience conducting clinical research at investigative sites as a clinical research coordinator and regulatory affairs specialist. Ten years of experience in the biopharmaceutical industry supporting clinical research by ensuring successful day to day clinical operations and support for regulatory submissions such as Investigational New Drug Applications, Drug Master Files, and 510ks. Knowledge and experience in the application of FDA guidelines and the US Code of Federal Regulations in relations to Current Good Clinical Practices (cGCP) and Current Good Manufacturing Practices (GMP). Current responsibilities include ensuring that all clinical trial projects are properly resourced, managed, and executed within budget and in accordance with established timelines and quality standards. Manage the day to day clinical operations, including the management of vendors and coordination of activities. Ensure that all clinical trials are executed in compliance with cGCP guidelines, FDA regulations, and company standard operating procedures. Resilience

Ccrp Angie Kimbler currently works in the
Resilience

Ccrp Angie Kimbler specializes in
Certified Clinical Research Professional (CCRP) with a BS in Clinical Research and over 20 years of experience in clinical research. Over ten years of experience conducting clinical research at investigative sites as a clinical research coordinator and regulatory affairs specialist. Ten years of experience in the biopharmaceutical industry supporting clinical research by ensuring successful day to day clinical operations and support for regulatory submissions such as Investigational New Drug Applications, Drug Master Files, and 510ks. Knowledge and experience in the application of FDA guidelines and the US Code of Federal Regulations in relations to Current Good Clinical Practices (cGCP) and Current Good Manufacturing Practices (GMP). Current responsibilities include ensuring that all clinical trial projects are properly resourced, managed, and executed within budget and in accordance with established timelines and quality standards. Manage the day to day clinical operations, including the management of vendors and coordination of activities. Ensure that all clinical trials are executed in compliance with cGCP guidelines, FDA regulations, and company standard operating procedures.

Ccrp Angie Kimbler speaks the following languages:
No languages available.

Ccrp Angie Kimbler has prior experience in the following industries:
Ology Bioservices , Nanotherapeutics , Nanotherapeutics , Nanotherapeutics , Nanotherapeutics , Amk Research , Clin Sci International

Ccrp Angie Kimbler has the following professional experience:
Resilience , Ology Bioservices , Nanotherapeutics , Nanotherapeutics , Nanotherapeutics , Nanotherapeutics , Amk Research , Clin Sci International .

You can view Ccrp Angie Kimbler’s
LinkedIn profile at LinkedIn URL.

Ccrp Angie Kimbler’s work email addresses are
[email protected].

Ccrp Angie Kimbler works at
Resilience

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